酿酒酵母XVI染色体38千碱基区功能分析

Sophia Ushinsky, Howard Bussey, Alia Ahmed, Ying Wang, James Friesen, Reginald Storms
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引用次数: 1

摘要

在本报告中,我们评估了酿酒酵母XVI染色体右臂上紧挨着着丝粒的38780碱基对区域内16个开放阅读框(orf)的功能重要性。该分析包括用编码来自维多利亚Aequorea水母和HIS3的绿色荧光蛋白的盒式磁带替换二倍体菌株中每个ORF的一个拷贝。每个替代盒通过PCR生成,使用45个碱基延伸的寡核苷酸对与目标基因编码区上游和下游的序列互补。在替换目标基因后,对每个基因替换菌株进行一系列遗传和表型测试,以评估删除基因的功能重要性。这一分析表明,两个orf是必不可少的,一个用于孢子萌发,另一个用于营养生长。第三个基因编码了铜拳状的转录因子,这是正确的芽位选择所必需的。16个orf中有一个是重复的,这种情况在用于酵母基因组测序的菌株(S288C)中没有观察到。RNA分析显示,该区域16个orf中有11个表达稳态poly(A+) RNA水平大于或等于酵母肌动蛋白基因ACT1表达水平的2%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional analysis of a 38 kilobase region on chromosome XVI inSaccharomyces cerevisiae

In this report we assess the functional importance of 16 open reading frames (ORFs) contained within a 38 780 base-pair region immediately adjacent to the centromere on the right arm of chromosome XVI in Saccharomyces cerevisiae. This analysis involved replacing one copy of each ORF in a diploid strain with a cassette encoding the green fluorescent protein from the jellyfish Aequorea victoria and HIS3. Each replacement cassette was generated by PCR using oligonucleotide pairs with 45-base extensions complementary to sequences immediately upstream and downstream of the target gene’s coding region. After replacement of the targeted genes, each gene-replacement strain was subjected to a series of genetic and phenotypic tests to assess the functional importance of the deleted gene. This analysis showed that two ORFs were essential, one for spores to germinate and another for vegetative growth. A third gene encoded a copper-fist-like transcription factor that was required for proper bud-site selection. One of the 16 ORFs was duplicated, a situation not observed in the strain used to sequence the yeast genome (S288C). RNA analysis showed 11 of the 16 ORFs in this region expressed steady-state poly(A+) RNA levels that were greater than or equal to 2% of the level expressed from the yeast actin gene, ACT1.

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